Compile Data Set for Download or QSAR
Found 88 with Last Name = 'retailleau' and Initial = 'p'
LigandPNGBDBM50569703(CHEMBL4851703)copy SMILES
Affinity DataKi:  280nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569685(CHEMBL4877631)copy SMILES
Affinity DataKi:  730nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569681(CHEMBL4867398)copy SMILES
Affinity DataKi:  1.15E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569680(CHEMBL4862416)copy SMILES
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569686(CHEMBL4868540)copy SMILES
Affinity DataKi:  1.40E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569689(CHEMBL4855728)copy SMILES
Affinity DataKi:  1.55E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569696(CHEMBL4867248)copy SMILES
Affinity DataKi:  1.58E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569690(CHEMBL4876416)copy SMILES
Affinity DataKi:  1.77E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569699(CHEMBL4855195)copy SMILES
Affinity DataKi:  1.81E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569698(CHEMBL4855265)copy SMILES
Affinity DataKi:  1.84E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569692(CHEMBL4864504)copy SMILES
Affinity DataKi:  1.89E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569688(CHEMBL4848727)copy SMILES
Affinity DataKi:  1.93E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569697(CHEMBL4860974)copy SMILES
Affinity DataKi:  1.96E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569687(CHEMBL4862171)copy SMILES
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569691(CHEMBL4866009)copy SMILES
Affinity DataKi:  2.36E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569684(CHEMBL4865343)copy SMILES
Affinity DataKi:  2.41E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569683(CHEMBL4849406)copy SMILES
Affinity DataKi:  3.60E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569679(CHEMBL4855927)copy SMILES
Affinity DataKi:  3.60E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569682(CHEMBL4849131)copy SMILES
Affinity DataKi:  3.60E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569702(CHEMBL4864325)copy SMILES
Affinity DataKi:  3.69E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569704(CHEMBL4848912)copy SMILES
Affinity DataKi:  3.89E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569694(CHEMBL4876790)copy SMILES
Affinity DataKi:  3.94E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569705(CHEMBL4853896)copy SMILES
Affinity DataKi:  4.15E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569695(CHEMBL4875502)copy SMILES
Affinity DataKi:  5.23E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295298(CHEMBL552717 | icterogenin regioisomer)copy SMILEScopy InChI
Affinity DataKi:  5.30E+3nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
LigandPNGBDBM50569701(CHEMBL4872507)copy SMILES
Affinity DataKi:  5.66E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569693(CHEMBL4854293)copy SMILES
Affinity DataKi:  6.04E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
LigandPNGBDBM50569700(CHEMBL4872541)copy SMILES
Affinity DataKi:  6.49E+3nMAssay Description:Inhibition of KPC-2 (unknown origin) expressed in Escherichia coli BL21 (DE3) incubated for 3 mins by spectrophotometric analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26977C2PubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295299(1-O-[alpha-L-(Rhamnopyranosyl]-23-acetoxy-3beta-ac...)copy SMILEScopy InChI
Affinity DataKi:  7.20E+3nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295300(CHEMBL554122 | icterogenin)copy SMILEScopy InChI
Affinity DataKi:  7.60E+3nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295301(23-O-[alpha-L-(2',4'-Diacetylrhamnopyranosyl]imber...)copy SMILEScopy InChI
Affinity DataKi:  1.41E+4nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295302(23-acetoxy-3beta-acetylimberbic acid | CHEMBL53990...)copy SMILEScopy InChI
Affinity DataKi:  1.78E+4nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295305(23-O-[alpha-L-(4'-Acetylrhamnopyranosyl]-3beta-ace...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295304(23-O-[alpha-L-(3',4'-Diacetylrhamnopyranosyl]-3bet...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295303(23-Acetoxyimberbic acid 29-methyl ester | CHEMBL55...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295306(1-O-[alpha-L-(Rhamnopyranosyl]-23-acetoxyimberbic ...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295307(23-O-[alpha-L-(4'-acetylrhamnopyranosyl]imberbic a...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295308(1-O-[alpha-L-(Rhamnopyranosyl]-23-acetoxy-3beta-ac...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295311(CHEMBL555367 | lantadene B)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295310(CHEMBL540988 | lantadene A)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetBcl-2-like protein 1(Homo sapiens (Human))
CNRS

Curated by ChEMBL
LigandPNGBDBM50295309(23-O-[alpha-L-(4'-Acetylrhamnopyranosyl]-3beta-ace...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Binding affinity to Bcl-xL by fluorescein-labeled Bak-BH3 peptide competition binding assayChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KH0NCVPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383311(CHEMBL2029619)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383305(CHEMBL2029615)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMedDrugBank
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383306(CHEMBL2029618)copy SMILEScopy InChI
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383304(CHEMBL2029622)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetDual specificity tyrosine-phosphorylation-regulated kinase 1A(RAT)
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM5655(2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 300nMAssay Description:Inhibition of GST-tagged rat recombinant DYRK1A expressed in Escherichia coli using KKISGRLSPIMTEQ as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383304(CHEMBL2029622)copy SMILEScopy InChI
Affinity DataIC50: 520nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383306(CHEMBL2029618)copy SMILEScopy InChI
Affinity DataIC50: 570nMAssay Description:Inhibition of human recombinant CDK5/p25 using [gamma 33P]ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
TargetDual specificity protein kinase CLK1(Mus musculus)
Institut de Chimie des Substances Naturelles (ICSN)

Curated by ChEMBL
LigandPNGBDBM50383311(CHEMBL2029619)copy SMILEScopy InChI
Affinity DataIC50: 670nMAssay Description:Inhibition of GST-tagged mouse recombinant CLK1 expressed in Escherichia coli using GRSRSRSRSRSR as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29W0GHWPubMed
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